Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype

Natural history of Barth syndrome: a national cohort study of 22 patients

(2013) Charlotte Rigaud et al.   Orphanet Journal of Rare Diseases

Barth syndrome

(2013) Sarah LN Clarke et al.   Orphanet Journal of Rare Diseases

The Barth Syndrome Registry: Distinguishing disease characteristics and growth data from a longitudinal study

(2012) Amy E. Roberts et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Diagnosis of Barth syndrome using a novel LC-MS/MS method for leukocyte cardiolipin analysis

(2012) Ann Bowron et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Cardiac and Skeletal Muscle Defects in a Mouse Model of Human Barth Syndrome

(2010) Devrim Acehan et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The 3-methylglutaconic acidurias: what’s new?

(2010) Saskia B. Wortmann et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth

(2010) C. G. Steward et al.   PRENATAL DIAGNOSIS

Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography–mass spectrometry as a diagnostic test for Barth syndrome

(2009) Riekelt H. Houtkooper et al.   ANALYTICAL BIOCHEMISTRY

Dysmorphology of Barth syndrome

(2009) Rob Hastings et al.   CLINICAL DYSMORPHOLOGY